聚苯胺/涤纶导电织物再掺杂及洗涤性能的研究

采用现场吸附聚合法制备了聚苯胺 /涤纶导电织物 ,采用不同种类的酸对其进行再掺杂 ,研究了酸的种类对织物导电性能的影响 ,并对导电织物进行了洗涤实验及洗涤牢度实验。结果表明 :无机酸对导电织物的掺杂效果优于大多数有机酸。导电涤纶织物的导电性能受洗涤液酸碱度的影响 ,其中碱性洗涤液使导电性能降低 2个数量级 ,酸性洗涤液使导电性能下降 1个数量级 ,而且聚苯胺在涤纶织物表面具有良好的附着性     

Preparation of conductive polyaniline/nanosilica particle composites through ultrasonic irradiation

Polyaniline/nano‐SiO₂ particle composites were prepared through ultrasonic irradiation. Polymerization of aniline was conducted under ultrasonic irradiation in the presence of two types of nano‐SiO₂: porous nanosilica and spherical nanosilica. The stability of the colloid dispersion, UV–vis spectra, composition, interaction, conductivity, and other characteristics of the composites were examined. It was found that the aggregation of nano‐SiO₂ could be reduced under ultrasonic irradiation and that nanoparticles were redispersed in the aqueous solution. The formed polyaniline deposited on the surface of the nanoparticle, which led to a core–shell structure. Two particle morphologies, threadlike aggregates with a few spherical nanoparticles for porous nanosilica and spherical particles with a few sandwichlike particles for spherical nanosilica, were observed. X‐ray photoelectron spectroscopy showed that for two types of composites the ratio of Si atoms to N atoms (Si:N) on the surface was much higher than that in the bulk. The UV–vis spectra of the diluted colloid dispersion of polyaniline/nano‐SiO₂ composite particles were similar to those of the polyaniline system. Fourier transform infrared spectroscopy suggested strong interaction between polyaniline and nano‐SiO₂. The conductivity of the polyaniline/porous nanosilica (23.1 wt % polyaniline) and polyaniline/spherical nanosilica (20.6 wt % polyaniline) composites was 2.9 and 0.2 S/cm, respectively. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 87: 1811–1817, 2003     

Tribological behaviors of hybrid PTFE/nomex fabric/phenolic composite reinforced with multiwalled carbon nanotubes

Modification of composites was a general method to improve their tribological behaviors. On the way to explore composites with enhanced tribological behaviors, we have successfully prepared hybrid PTFE/Nomex fabric/phenolic composite filled with multiwalled carbon nanotubes (MWCNTs) or MWCNTs modified by polystyrene (PS) with a grafting to method. The results of pin‐on‐disc type wear tests indicated tribological behaviors were improved both for hybrid PTFE/Nomex fabric/phenolic composite filled with MWCNTs and MWCNTs‐PS, especially for that of filled with MWCNTs‐PS. And the probable reason was also discussed based on the characterization results. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Effect of conductive polyaniline in thermoplastic natural rubber blends on the mechanical,thermal stability,and electrical conductivity properties

This research was conducted to fabricate thermoplastic natural rubber/polyaniline (TPNR/PANI) blends via melt blending method using an internal mixer and followed by compression molding. The effects of PANI contents between 1 and 5 wt % PANI in the TPNR blends on the mechanical properties, thermal stability, electrical conductivity (impedance), and morphology observation were investigated. The TPNR/3 wt % PANI sample exhibited the highest tensile strength (3.7 MPa), elongation at break (583%), flexural strength (1.8 MPa), flexural modulus (37.0 MPa), and impact strength (7.1 kJ m⁻²). From the aspect of thermal properties, it was found that with the addition of PANI, the thermal stability of the TPNR/PANI increased. Comparing to nonconductive TPNR sample, the incorporation of PANI promoted the electrical conductivity characteristic to PANI-filled TPNR blends which showing a magnitude order of 10⁻⁹ S cm⁻¹. Scanning electron microscopy micrograph revealed the good distribution of PANI at the optimum content (3 wt % PANI) in the TPNR blends and the good interaction between TPNR and PANI. It can be concluded that the TPNR blends incorporated with a low loading of PANI could be a newly good conductive material. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47527.     

导电聚苯胺在电流变液中的应用

简述了电流变液的研究现状,着重介绍了含聚苯胺粒子电流变液的应用现状及发展前景。     

导电聚苯胺高分子复合材料的研究进展

重点介绍了聚苯胺结构与性能，综述了聚苯胺高分子复合材料的应用及其制备方法．水溶性聚苯胺的研究进展，并展望了聚苯胺复合材料具有广阔的应用前景。该工作对于全面了解聚苯胺具有一定的意义。     

Polypyrrole/polyaniline conductive films obtained electrochemically on polycarbonate‐coated platinum electrodes

In this study, two‐component free‐standing films were obtained by coating a polycarbonate (PC)‐coated Pt electrode first with polypyrrole (PPy) in an organic medium and then polyaniline (PAn) in an aqueous medium using an electrochemical technique. The amount of PPy and PAn contained in the films was controlled by varying the electrolysis time. The PC/PPy/PAn films were characterized by cyclic voltammetry, conductivity, FTIR and UV–visible spectrophotometry, and thermogravimetric analysis. The resistance change of the films was determined in the temperature range of ?15 to 120 °C and their temperature sensor properties were investigated. © 2002 Society of Chemical Industry     

Synthesis and characterization of polyacrylamide–polyaniline conductive blends

Conducting poly(acrylamide) films were synthesized by exposing the polyacrylamide films impregnated with ammonium peroxodisulphate, an oxidizing agent, to hydrochloric acid vapor and then to aniline vapor. The effects of varying the exposure time to aniline vapor and the resulting composite films of polyacrylamide–polyaniline were characterized by different methods. The mode of conduction has also been studied. The conductivity of the resulting composites reached up to 10⁻⁵ s/cm². © 1998 John Wiley & Sons, Inc. J Appl Polym Sci 69: 841–844, 1998     

聚苯胺及其导电阻燃涤纶的制备

采用氧化聚合的方法合成聚苯胺,并考察了不同温度下聚苯胺的产率和电导率,探讨了阻燃涤纶碱减量处理条件,用原位聚合的方法制备聚苯胺/阻燃涤纶导电纤维。结果表明,在-20℃下合成的聚苯胺产率较高为84%,电导率为124 S/cm。阻燃涤纶碱减量处理的适宜条件为:温度80℃,碱浓度为5%,处理时间15-20 min,低温下制备的聚苯胺/阻燃涤纶失重为2.50%-5.25%时,纤维的电导率提高得较快,为0.07-0.13 S/cm。     

聚苯胺/聚酰胺导电初生纤维形态结构的研究

以聚苯胺 ( PANI)为导电组分 ,聚酰胺 -11为基体 ,浓硫酸为溶剂制备纺丝浆液 ,采用湿法纺丝路线纺制导电纤维。当 PAN I在纤维中的质量分数为 5 %和 12 %时 ,纤维的电导率分别提高到10 -5S/ cm和 10 -2 S/ cm。采用扫描电子显微镜 ( SEM)研究了凝固浴中酸的含量以及纺丝浆液中 PANI的含量对初生纤维形态结构的影响 ,并探讨了初生纤维的微观结构对纤维的拉伸性能的影响     

聚苯胺/乙炔炭黑多孔类棒状复合材料的制备及电化学性质

以纳米乙炔炭黑在盐酸掺杂的反应体系中的聚集体为硬模板,原位吸附化学氧化法制备了聚苯胺/炭黑复合材料。实验结果显示,聚苯胺复合物为表面附着大量纳米颗粒的类棒状结构,且棒与棒间富有孔隙。复合材料分解温度在350℃左右。循环伏安曲线表现出该复合材料法拉第准(赝)电容有良好的电极可逆性,在5,10 mA/cm2电流密度下,单电极比电容高达376 F/g和311 F/g。     

Effect of dopant and oxidant on the electrochemical properties of polyaniline/graphite nanoplate composites

Optimizing the synthesis parameters of polyaniline/graphite nanoplate (PANI/GNP) composite is essential to the final electrochemical performance. Herein, the electrochemical properties of PANI/GNP composites, prepared by in situ chemical polymerization using varying amounts of different oxidants, with or without the addition of 4‐dodecylbenzenesulfonic acid (DBSA) as dopant, were investigated. Cyclic voltammetric results suggested that a stoichiometric amount of the oxidant iron chloride (FeCl₃) was beneficial to the electrochemical properties of the composites. The use of ammonium persulfate (APS) instead of FeCl₃ as oxidant largely increased the actual PANI content, conductivity and specific capacitance of the PANI/GNP composites. The dopant DBSA increased the conductivity of the PANI/GNP composites but did not show a positive effect on the electrochemical behavior. The cyclic voltammograms of the PANI/GNP composites indicated that the pseudocapacitance of PANI contributes more than the electrical double‐layer capacitance of GNP to the capacitance of the composites, while the presence of GNP plays an essential role in the rate capability of the composites. In this study, PANI/GNP (1:1) composite synthesized with an APS to aniline molar ratio of 1 showed a balanced combination of high specific capacitance (180.5 F g^?1 at 20 mV s^?1) and good rate capability (78% retention at 100 mV s^?1). © 2018 Society of Chemical Industry     

含导电聚苯胺类锂离子电池复合材料的现状及发展趋势

导电聚苯胺（PANI）是近十年来研究最多的导电聚合物,具有比容量高、氧化还原可逆性好、电导率高、合成方法简单、成本低等特点,在化学电源和超级电容器中的应用最为广泛。导电聚苯胺复合材料的合成方法主要分为：原位复合法、共混法、自组装和电化学复合法等。导电聚苯胺复合材料可作为高能物质用于研发电极材料,但目前利用导电聚苯胺对锂离子电池三元正极材料进行修饰改性的研究较少。综述了导电聚苯胺及其复合材料的热电化学性能,重点对导电聚苯胺/锂离子电池复合正极材料的性能进行了阐述。最后对导电聚苯胺复合材料的应用和研究方向进行了总结,并简述了导电聚苯胺包覆改性LiNi_1-x-yCo_xMn_yO₂复合材料的应用和展望。     

聚苯胺/磺化EPDM锌离聚体导电复合物的制备与性能

在十二烷基苯磺酸存在下，用原位乳液聚合技术聚合苯胺，制得了聚苯胺和磺化乙丙橡胶（EPDM）锌离聚体复合物，EPDM锌离聚体由EPDM磺化及中和制得。用磺化度分别为0.10,0.24,0.40mmol/g的EPDM锌离聚体作为基质制备出各自的复合物，复合物可以熔融热塑加工，其导电率呈现的渗滤阈值为13%，在聚苯胺质量分数相同的情况下，磺化度小的复合物的电导率高于磺化度大的复合物。当磺化度为0.10mmol/g、聚苯胺质量分数为6%～11%和磺化度为0.24mmol/g、聚苯胺质量分数为2%～11%时，复合物表现出热塑性弹性体的行为，扯断伸长率达200%～500%，永久变形小于40%，用间甲酚进行二次掺杂后复合物的电导率有所提高，加入硬脂酸锌会降低复合物的电导率及力学性能。     

Effect of drying conditions on microwave conductivity of polyaniline

Polyaniline was synthesized by using ammonium persulfate initiator in the presence of 1M HCl. It was dried under different drying conditions like room temperature drying (for 48 h), oven drying (at 50–60°C for 8 h under a vacuum), and vacuum drying (at room temperature for 16 h). The conductivities of these samples were measured at microwave frequencies. These samples were also pelletized and the measurements were repeated. The cavity perturbation technique was used for the study. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 83: 2008–2012, 2002     

Effect of water on inorganic acids doped polyaniline

Based on gravimetric measurements, the effect of water on thin films of inorganic acids doped polyaniline (PANI) was developed. The starting point was the fact that PANI coating on the electrode of quartz crystal microbalances (QCM) showed significant frequency shifts under exposure to liquid water. The changes in the frequency as a function of treatment time in water were quantitatively measured. These changes suggested that the mass decreases under water exposure were due to dopant ions release. The data have been collected using doped PANI films with HCl, H₂SO₄, and H₃PO₄. For PANI‐HCl upon immersion in water showed rapid mass loss followed by slow kinetically dopant ions release with time. However, PANI‐H₃PO₄ and PANI‐H₂SO₄ showed a slow kinetically release out of the film immediately upon immersion in water. The release process was well described by Fickian diffusion process. The diffusion coefficients (D) were determined and found to be dependent on the acid dopant utilized. They varied within the range of (1.68–14.7) × 10^‐14 cm²/s. This work presented an attempt to find a simple method based on the QCM for investigating the diffusion of dopant ions out of thin PANI films upon immersion in water and determining D. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

Facile preparation of conductive paint made with polyaniline/dodecylbenzenesulfonic acid dispersion and poly(methyl methacrylate)

We investigated an easy way to prepare industrially a conductive paint made with polyaniline (PANI)/dodecylbenzenesulfonic acid (DBSA) dispersion and poly(methyl methacrylate) (PMMA) in organic media. First, water‐dispersible PANI doped with DBSA was chemically synthesized with aniline sulfate using ammonium persulfate in water, and the resulting PANI/DBSA was readily extracted from the reaction medium with a mixture of toluene and methyl ethyl ketone (MEK) (toluene:MEK = 1:1 (v/v)), which is useful for industrial applications. The obtained PANI/DBSA organic dispersion was mixed with PMMA organic solution to give the corresponding PANI/DBSA conductive paint containing PMMA. A film prepared with the resulting PANI/DBSA conductive paint was found to possess relatively good conductivity and low surface resistivity for a conductive paint utilized for an electrostatic discharge even at low PANI/DBSA content in the PANI/DBSA–PMMA composite film (the conductivity and the surface resistivity were 9.48 × 10^?4 S cm^?1 and 3.14 × 10⁶ Ω cm^?2, respectively, when the feed ratio of PANI/DBSA:PMMA was 1:39 (w/w)). Furthermore, it was found that the conductivity of the film composed of PANI/DBSA–PMMA composite can be readily and widely controlled by the PANI/DBSA content of the composite or by the amount of DBSA used during the PANI/DBSA synthesis. The highest conductivity of PANI/DBSA–PMMA composite film (7.84 × 10^?1 S cm^?1) was obtained when the feed ratio of PANI/DBSA:PMMA was 1:4 (w/w). Copyright © 2007 Society of Chemical Industry     

Preparation of conductive polyaniline/chlorosulfonated polyethylene composites via in situ emulsion polymerization and study of their properties

The conductive composites of polyaniline (PAn) and chlorosulfonated polyethylene (CSPE) were prepared by polymerization of aniline in the presence of CSPE, using a direct, one‐step in situ emulsion polymerization method. The polymerization of aniline was performed in an emulsion comprising water and xylene containing CSPE in the presence of dodecylbenzene sulfonic acid, which acts both as a surfactant and a dopant for PAn. The composites can be processed by either melt method (MP) or solution method (SP). Conductivity of the composites obtained by different processing methods shows different percolation thresholds: 14 wt % for MP samples and 22 wt % for SP samples. At the same content of PAn, the conductivity of MP composites is higher than that of SP composites. The relationships between mechanical properties and PAn content obtained by the two different processing methods were also investigated. When PAn content of MP samples is between 12 and 18 wt %, the composites behave like a thermoplastic elastomer with tensile strength at 6–8 MPa, ultimate elongation > 400% and permanent set < 30%. The conductivity of composites obtained by SP method after secondary doping with m‐cresol is about 6 orders of magnitude higher than the original at below 18 wt % PAn content and the percolation threshold for conductivity is lowered to 3 wt % PAn content. The composite shows no electrochromic activity in acidic solution of LiClO₄ in propylene carbonate, but after secondary doping exhibits electrochromic activity even in neutral electrolyte. © 2000 John Wiley & Sons, Inc. J Appl Polym Sci 76: 845–850, 2000     

Effect of annealing on electrical conductivity and morphology of polyaniline films

We report structure–property relationships of polyaniline emeraldine base (EB) films that were produced by combining different processing steps in various sequences. The effect of annealing and doping processes on the surface structure of the films was investigated by atomic force microscopy (AFM), and the corresponding changes to the chemical structure of the EB films were monitored by Fourier transform infrared spectroscopy. AFM results indicate that after doping polyaniline (EB) films with HCl, the root mean square (rms) roughness of the surface of EB film increased ～ 46%. When the doped films were annealed at 180°C under a nitrogen atmosphere for 3 h, the rms roughness was essentially unchanged from that of the initial, undoped films. The electrical conductivity of the films also showed a significant dependence on the processing sequence. When the doped polyaniline (EB) films were annealed, no electrical conductivity was observed. When these films were redoped, only ～ 6% of the initial conductivity could be recovered. In another processing sequence in which the polyaniline (EB) films were first annealed and then doped, the electrical conductivity was only ～ 12% relative to the film that was doped immediately after being cast. From this work, a strategy to reduce the surface roughness of films made from electrically conducting polyaniline (EB) is proposed. © 2001 John Wiley & Sons, Inc. J Appl Polym Sci 82: 3602–3610, 2001     

Electrical and structural analysis of conductive polyaniline/polyimide blends

Conducting films of dodecylbenzenesulfonic (DBSA)‐doped polyaniline/polyimide (PANI/PI) blends with various compositions were prepared by solvent casting followed by a thermal imidization process. Electrical and physical properties of the blends were characterized by infrared spectroscopy, an X‐ray diffraction technique, thermal analysis, a UV‐vis spectrophotometer, a dielectrometer, and conductivity measurements. The blends exhibited a relatively low percolation threshold of electrical conductivity at 5 wt % PANI content and showed higher conductivity than that of pure DBSA‐doped PANI when the PANI content exceeded 20 wt %. A lower percolation threshold and a lower compatibility was shown between the two components in the blends than those of PANI–camphorsulfonic acid/polyamic acid (PANI–CSA/PAA). A well‐defined layered structure due to the alignment of the long alkyl chain dopant perpendicular to the PANI main chain was evidenced by WAXD spectra. © 1999 John Wiley & Sons, Inc. J Appl Polym Sci 71: 2169–2178, 1999